ClinVar Miner

List of variants in gene POLG reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 34
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HGVS dbSNP
NM_002693.2(POLG):c.-160+6C>T rs886051526
NM_002693.2(POLG):c.-170T>A rs796052915
NM_002693.2(POLG):c.-241C>T rs886051527
NM_002693.2(POLG):c.-67A>G rs553331485
NM_002693.2(POLG):c.-80C>T rs3087378
NM_002693.2(POLG):c.1156C>T (p.Arg386Cys) rs199759055
NM_002693.2(POLG):c.1170+6G>A rs749250690
NM_002693.2(POLG):c.1171-11C>T rs886051525
NM_002693.2(POLG):c.1386G>A (p.Ser462=) rs62640034
NM_002693.2(POLG):c.1585+11T>C rs201566815
NM_002693.2(POLG):c.1743C>T (p.Asp581=) rs140743000
NM_002693.2(POLG):c.1887C>T (p.Asp629=) rs886051524
NM_002693.2(POLG):c.1902G>T (p.Leu634=) rs886051523
NM_002693.2(POLG):c.1905G>A (p.Pro635=) rs550592814
NM_002693.2(POLG):c.2028G>A (p.Ala676=) rs373550219
NM_002693.2(POLG):c.2071-14T>G rs150088708
NM_002693.2(POLG):c.2157+11C>T rs56411159
NM_002693.2(POLG):c.2157+15G>A rs766521182
NM_002693.2(POLG):c.2265+1G>C rs796052884
NM_002693.2(POLG):c.2266-11G>C rs747154432
NM_002693.2(POLG):c.2279G>A (p.Cys760Tyr) rs752878861
NM_002693.2(POLG):c.2481-10A>C rs555280530
NM_002693.2(POLG):c.2601T>C (p.Pro867=) rs201749977
NM_002693.2(POLG):c.3131T>C (p.Val1044Ala) rs150233690
NM_002693.2(POLG):c.3197C>T (p.Thr1066Met) rs750794449
NM_002693.2(POLG):c.3198G>A (p.Thr1066=) rs61752780
NM_002693.2(POLG):c.3273+6T>A rs886051522
NM_002693.2(POLG):c.3334A>T (p.Met1112Leu) rs767168260
NM_002693.2(POLG):c.3482+6C>T rs55779802
NM_002693.2(POLG):c.3549C>T (p.Val1183=) rs777231247
NM_002693.2(POLG):c.3561G>C (p.Arg1187=) rs62640037
NM_002693.2(POLG):c.452T>C (p.Leu151Pro) rs749018627
NM_002693.2(POLG):c.798G>T (p.Val266=) rs143631183
NM_002693.2(POLG):c.830A>T (p.His277Leu) rs138929605

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